Quality Assurance Specialist
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Our client, a leading international company, is seeking a Quality Engineer to strengthen their quality team. Based in the Kontich region of Belgium, this role involves quality assurance of development projects, including supplier qualification and risk management.
* Key Responsibilities:
* Lead design and development activities to meet regulatory requirements.
* Perform supplier qualification processes, ensuring compliance with ISO 13485, MDR, and ISO 14971.
* Plan, conduct, and document supplier audits to assess adherence to relevant standards.
Requirements:
* A Master's degree in Engineering, Life Sciences, Pharmacy, or a related field, or a proven track record in the related field.
* At least 5 years of experience in Quality Engineering or Supplier Quality within the medical device industry (pharmaceutical experience is a plus).
* Strong knowledge of ISO 13485, MDR, ISO 14971, and any additional country regulations or knowledge of GMP.
About Us:
We are a global life science recruitment firm specializing in partnering with start-ups and fast-growing biotech and pharmaceutical organizations.
We provide a quality-based approach to contingent search, tapping into our network of contacts to find the best talent for your organization.